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单个突触终末中存在高亲和力和低亲和力二磷酸五核苷酸诱导的钙反应,且与P2X1 - 7亚基的分布缺乏相关性。

Existence of high and low affinity dinucleotides pentaphosphate-induced calcium responses in individual synaptic terminals and lack of correlation with the distribution of P2X1-7 subunits.

作者信息

Gómez-Villafuertes R, Sánchez-Nogueiro J, Marín-García P, Miras-Portugal M T

机构信息

Departamento de Bioquímica, Facultad de Veterinaria, Universidad Complutense de Madrid, Av. Puerta de Hierro s/n, 28040 Madrid, Spain; Centro Nacional de Biotecnología, C.S.I.C., 28049 Madrid, Spain.

出版信息

Neurochem Int. 2007 Mar;50(4):628-41. doi: 10.1016/j.neuint.2006.12.007. Epub 2006 Dec 21.

DOI:10.1016/j.neuint.2006.12.007
PMID:17229490
Abstract

Individual analysis of synaptic terminals calcium responses, induced by dinucleotides pentaphosphate, Ap(5)A or Gp(5)G, demonstrates the presence of two main groups considering the concentration required for stimulation. The first group corresponds to those responding to Ap(5)A or Gp(5)G at nanomolar concentration, representing 16% and 12%, respectively, and the second one responds to micromolar concentration and represents, respectively, 17% and 14%, of the total functional synaptosomal population in rat midbrain. Dose-response curves in single terminals showed an Ap(5)A EC(50) values of 0.9+/-0.2 nM and 11.8+/-0.9 microM, being the maximal intrasynaptosomal calcium increase of 200+/-0.3 and 125+/-0.2 nM for the high and low affinity responding terminals, respectively. Combination of microfluorimetric and immunocytochemical studies showed lack of correlation between dinucleotides pentaphosphate responses and P2X receptor subunits expression, in spite of the abundance of P2X(2), P2X(3) and P2X(7) at the presynaptic level in rat midbrain synaptosomes. Pyridoxalphosphate-6-azophenyl-2',4'-disulfonic acid (PPADS), a P2X receptors antagonist, showed no effect on low affinity dinucleotides receptors population, and partial inhibition on the high affinity one. On the other hand, diinosine pentaphosphate (Ip(5)I) completely abolished the low affinity dinucleotides responses, and 60% inhibition of the high affinity ones.

摘要

对由二磷酸五核苷酸、Ap(5)A或Gp(5)G诱导的突触终末钙反应进行的个体分析表明,考虑到刺激所需的浓度,存在两个主要组。第一组对应于那些对纳摩尔浓度的Ap(5)A或Gp(5)G有反应的突触终末,分别占大鼠中脑总功能性突触体群体的16%和12%,第二组对微摩尔浓度有反应,分别占17%和14%。单个终末的剂量反应曲线显示Ap(5)A的EC(50)值为0.9±0.2 nM和11.8±0.9 μM,对于高亲和力和低亲和力反应终末,突触体内钙的最大增加分别为200±0.3 nM和125±0.2 nM。微荧光测定和免疫细胞化学研究的结合表明,尽管大鼠中脑突触体的突触前水平存在大量P2X(2)、P2X(3)和P2X(7),但二磷酸五核苷酸反应与P2X受体亚基表达之间缺乏相关性。P2X受体拮抗剂磷酸吡哆醛-6-偶氮苯-2',4'-二磺酸(PPADS)对低亲和力二核苷酸受体群体没有影响,对高亲和力受体群体有部分抑制作用。另一方面,二肌苷五磷酸(Ip(5)I)完全消除了低亲和力二核苷酸反应,并对高亲和力反应有60%的抑制作用。

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